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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174933Generated: November 1, 2026

1-Methyl-4-(methylamino)piperidine → Methyl-(1-methyl-piperidin-4-yl)-(5-nitro-benzooxazol-2-yl)-amine

https://huagongshe.com/reaction/1174933

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-4-(methylamino)piperidineHCID 566323—
Reactant2-Ethylsulfanyl-5-nitrobenzooxazoleHCID 57421495—
ProductMethyl-(1-methyl-piperidin-4-yl)-(5-nitro-benzooxazol-2-yl)-amineHCID 59558006—

Reaction Steps

The title compound is prepared according to the procedure described in General Method A, using 2-ethylsulfanyl-5-nitrobenzooxazole (1.17 g, 5.23 mmol) and methyl-(1-methyl-piperidin-4-yl)-amine (1.37 mL, 9.42 mmol) in anhydrous THP (10 mL) at 100° C.: (0.608 g, 40%). mass spectrum (m/e): 291.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838543B2
Source datasetuspto-grants-2010_11
ORD IDord-15ba5111b4234b948c3f2f233bc5ee49
Source noteuspto-grants-2010_11